A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432630



Internal ID21090183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1106414..1832520hg38UCSC Ensembl
chr8:1056414..1780686hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38726107
hg19724273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231372
Samples
Known GenesARHGEF10, CLN8, DLGAP2, ERICH1-AS1, LOC100507435, LOC286083, MIR596
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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